Chinese Journal of Organic Chemistry ›› 2020, Vol. 40 ›› Issue (1): 115-124.DOI: 10.6023/cjoc201907050 Previous Articles     Next Articles


马奔a, 王刚刚a, 周红艳a,b, 杨靖亚a   

  1. a 西北师范大学化学化工学院 兰州 730070;
    b 甘肃农业大学理学院 兰州 730070
  • 收稿日期:2019-07-29 修回日期:2019-08-26 发布日期:2019-09-12
  • 通讯作者: 杨靖亚, 马奔;
  • 基金资助:

Alkali Salt-Catalyzed Aza-Michael Addition of 1,2,4-Triazole to α,β-Unsaturated Ketones and Imides

Ma Bena, Wang Gangganga, Zhou Hongyana,b, Yang Jingyaa   

  1. a College of Chemistry and Chemical Engineering, Northwest Normal University, Lanzhou 730070;
    b College of Science, Gansu Agricultural University, Lanzhou 730070
  • Received:2019-07-29 Revised:2019-08-26 Published:2019-09-12
  • Supported by:
    Project supported by the National Natural Science Foundation of China (No. 21362034).

An alkali salt-catalyzed highly efficient aza-Michael addition of 1,2,4-triazole to α,β-unsaturated ketones and imides has been developed, giving the desired products in moderate to excellent yields. The salient features of this reaction involve readily available starting materials, good substrate scope, mild condition, high efficiency and ease of scale-up. The product can be transformed into corresponding γ-aminoalcohol.

Key words: synthetic methods, Michael addition, enones, α,β-unsaturated imides, nitrogen heterocycles, 1,2,4-triazole